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Journal Abstract Search

124 related items for PubMed ID: 6980322

  • 1. Increased urinary excretion of total 16 alpha-hydroxypregnenolone in newborn infants with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Homoki J, Teller WM.
    Klin Wochenschr; 1982 Apr 15; 60(8):407-10. PubMed ID: 6980322
    [Abstract] [Full Text] [Related]

  • 2. Urinary excretion of 17-hydroxypregnanolones in patients with different forms of congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.
    Homoki J, Sólyom J, Wachter U, Teller WM.
    Eur J Pediatr; 1992 Jan 15; 151(1):24-8. PubMed ID: 1728539
    [Abstract] [Full Text] [Related]

  • 3. A paradox: elevated 21-hydroxypregnenolone production in newborns with 21-hydroxylase deficiency.
    Shackleton CH, Homoki J, Taylor NF.
    Steroids; 1987 Jan 15; 49(4-5):295-311. PubMed ID: 3502660
    [Abstract] [Full Text] [Related]

  • 4. Identification of 15 beta-hydroxylated C21 steroids in the neo-natal period: the role of 3 alpha,15 beta,17 alpha-trihydroxy-5 beta-pregnan-20-one in the perinatal diagnosis of congenital adrenal hyperplasia (CAH) due to a 21-hydroxylase deficiency.
    Joannou GE.
    J Steroid Biochem; 1981 Sep 15; 14(9):901-12. PubMed ID: 6975400
    [No Abstract] [Full Text] [Related]

  • 5. [Reevaluation of recalled infants by neonatal mass screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Diagnostic value of pregnanetriolone in a single urine specimen using glass capillary gas chromatography].
    Hikita Y.
    Nihon Naibunpi Gakkai Zasshi; 1985 Mar 20; 61(3):197-219. PubMed ID: 3874793
    [Abstract] [Full Text] [Related]

  • 6. Male pseudohermaphroditism due to multiple defects in steroid-biosynthetic microsomal mixed-function oxidases. A new variant of congenital adrenal hyperplasia.
    Peterson RE, Imperato-McGinley J, Gautier T, Shackleton C.
    N Engl J Med; 1985 Nov 07; 313(19):1182-91. PubMed ID: 2932643
    [Abstract] [Full Text] [Related]

  • 7. Diagnosis of 21-hydroxylase deficiency in newborn infants by GC-MS of urinary steroids.
    Yong AB, Pitt JJ, Montalto J, Davies HE, Warne GL, Connelly JF.
    Aust Paediatr J; 1988 Oct 07; 24(5):280-5. PubMed ID: 3265870
    [Abstract] [Full Text] [Related]

  • 8. Urinary excretion of pregnanetriol and 5 -pregnenetriol in two forms of congenital adrenal hyperplasia.
    Bongiovanni AM, Eberlein WR, Moshang T.
    J Clin Invest; 1971 Dec 07; 50(12):2751-4. PubMed ID: 5129323
    [Abstract] [Full Text] [Related]

  • 9. 11 Beta-hydroxylase deficiency congenital adrenal hyperplasia: update of prenatal diagnosis.
    Rösler A, Weshler N, Leiberman E, Hochberg Z, Weidenfeld J, Sack J, Chemke J.
    J Clin Endocrinol Metab; 1988 Apr 07; 66(4):830-8. PubMed ID: 3346360
    [Abstract] [Full Text] [Related]

  • 10. Pregnenolone, 17-OH-pregnenolone, and testosterone in plasma of patients with congenital adrenal hyperplasia.
    McKenna TJ, Jennings AS, Liddle GW, Burr IM.
    J Clin Endocrinol Metab; 1976 May 07; 42(5):918-25. PubMed ID: 178685
    [Abstract] [Full Text] [Related]

  • 11. Serum 17-hydroxypregnenolone and 17-hydroxypregnenolone sulfate concentrations in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Shimozawa K, Saisho S, Yata J, Kambegawa A.
    Endocrinol Jpn; 1988 Feb 07; 35(1):11-8. PubMed ID: 3260857
    [Abstract] [Full Text] [Related]

  • 12. Detection of late onset steroid 21-hydroxylase deficiency by capillary gas chromatographic profiling of urinary steroids in children and adolescents.
    Homoki J, Solyom J, Teller WM.
    Eur J Pediatr; 1988 Apr 07; 147(3):257-62. PubMed ID: 3260557
    [Abstract] [Full Text] [Related]

  • 13. Congenital adrenal hyperplasia caused by defect in steroid 21-hydroxylase. Establishment of definitive urinary steroid excretion pattern during first weeks of life.
    Shackleton CH.
    Clin Chim Acta; 1976 Mar 15; 67(3):287-98. PubMed ID: 1261045
    [Abstract] [Full Text] [Related]

  • 14. Difficulties in the diagnosis of congenital adrenal hyperplasia in early infancy: the 11 beta-hydroxylase defect.
    Honour JW, Anderson JM, Shackleton CH.
    Acta Endocrinol (Copenh); 1983 May 15; 103(1):101-9. PubMed ID: 6602444
    [Abstract] [Full Text] [Related]

  • 15. The diagnosis of 21-hydroxylase deficiency in a prematurely born infant on the basis of the urinary steroid excretion pattern.
    van der Ploeg KR, Wolthers BG, Nagel GT, Volmer M, Drayer NM.
    Clin Chim Acta; 1982 Apr 23; 120(3):341-53. PubMed ID: 6978779
    [Abstract] [Full Text] [Related]

  • 16. Congenital adrenal hyperplasia due to deficiency of 11 -hydroxylation of 17 -hydroxylated steroids.
    Zachmann M, Völlmin JA, New MI, Curtius HC, Prader A.
    J Clin Endocrinol Metab; 1971 Sep 23; 33(3):501-8. PubMed ID: 4328339
    [No Abstract] [Full Text] [Related]

  • 17. A pilot study for neonatal screening of congenital adrenal hyperplasia due to 21-hydroxylase and 11-beta-hydroxylase deficiency in Campania region.
    Valentino R, Tommaselli AP, Rossi R, Lombardi G, Varrone S.
    J Endocrinol Invest; 1990 Mar 23; 13(3):221-5. PubMed ID: 2365957
    [Abstract] [Full Text] [Related]

  • 18. [Connection between congenital adrenal hyperplasia due to 21-hydroxylase deficiency and the HLA genotype].
    Dumić M, Brkljacić L, Krzisnik C, Radica A, Tajić M, Kastelan A.
    Lijec Vjesn; 1983 Mar 23; 105(7-8):290-2. PubMed ID: 6605467
    [No Abstract] [Full Text] [Related]

  • 19. Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasia.
    Levine LS, Dupont B, Lorenzen F, Pang S, Pollack M, Oberfield S, Kohn B, Lerner A, Cacciari E, Mantero F, Cassio A, Scaroni C, Chiumello G, Rondanini GF, Gargantini L, Giovannelli G, Virdis R, Bartolotta E, Migliori C, Pintor C, Tato L, Barboni F, New MI.
    J Clin Endocrinol Metab; 1980 Dec 23; 51(6):1316-24. PubMed ID: 6449518
    [Abstract] [Full Text] [Related]

  • 20. Combined 21- and 11 beta-hydroxylase deficiency in familial congenital adrenal hyperplasia.
    Hurwitz A, Brautbar C, Milwidsky A, Vecsei P, Milewicz A, Navot D, Rösler A.
    J Clin Endocrinol Metab; 1985 Apr 23; 60(4):631-8. PubMed ID: 2982904
    [Abstract] [Full Text] [Related]

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